Variant report

Variant	nsv542902
Chromosome Location	chr16:31337455-31414881
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1331)
CpG islands
(count:2077)
Chromatin interactive
region (count:65)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1331 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:31366319-31366447	K562	blood:	n/a	n/a
2	ARID3A	chr16:31393918-31394149	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:31358850-31359040	K562	blood:	n/a	n/a
4	ARID3A	chr16:31383068-31383352	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:31345139-31345361	HepG2	liver:	n/a	n/a
6	ATF1	chr16:31397640-31398214	K562	blood:	n/a	n/a
7	ATF2	chr16:31365790-31366176	GM12878	blood:	n/a	n/a
8	ATF2	chr16:31355941-31356677	GM12878	blood:	n/a	n/a
9	ATF2	chr16:31376334-31376899	GM12878	blood:	n/a	n/a
10	ATF2	chr16:31365534-31366644	GM12878	blood:	n/a	n/a
11	ATF2	chr16:31362818-31363253	GM12878	blood:	n/a	n/a
12	ATF2	chr16:31362642-31363600	GM12878	blood:	n/a	n/a
13	ATF2	chr16:31356015-31356477	GM12878	blood:	n/a	n/a
14	BACH1	chr16:31345007-31345368	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr16:31378233-31378510	GM12878	blood:	n/a	n/a
16	BATF	chr16:31366208-31366628	GM12878	blood:	n/a	n/a
17	BATF	chr16:31365677-31366080	GM12878	blood:	n/a	n/a
18	BATF	chr16:31358709-31359032	GM12878	blood:	n/a	chr16:31358870-31358881
19	BATF	chr16:31356052-31356507	GM12878	blood:	n/a	n/a
20	BATF	chr16:31355994-31356532	GM12878	blood:	n/a	n/a
21	BCL11A	chr16:31365702-31366108	GM12878	blood:	n/a	n/a
22	BCL11A	chr16:31362727-31363125	GM12878	blood:	n/a	chr16:31362914-31362923 chr16:31363095-31363104
23	BCL11A	chr16:31355939-31356505	GM12878	blood:	n/a	chr16:31356243-31356252
24	BCL11A	chr16:31356001-31356366	GM12878	blood:	n/a	chr16:31356243-31356252
25	BCL11A	chr16:31362856-31363088	GM12878	blood:	n/a	chr16:31362914-31362923
26	BCL3	chr16:31340650-31340957	GM12878	blood:	n/a	n/a
27	BCL3	chr16:31342980-31343556	GM12878	blood:	n/a	n/a
28	BCL3	chr16:31339430-31340482	GM12878	blood:	n/a	n/a
29	BCL3	chr16:31342861-31343532	GM12878	blood:	n/a	n/a
30	BCL3	chr16:31339512-31340343	GM12878	blood:	n/a	n/a
31	BCLAF1	chr16:31365629-31366459	GM12878	blood:	n/a	n/a
32	BCLAF1	chr16:31356010-31356569	GM12878	blood:	n/a	chr16:31356243-31356252
33	BCLAF1	chr16:31362617-31363369	GM12878	blood:	n/a	chr16:31362914-31362923 chr16:31363095-31363104
34	BCLAF1	chr16:31355875-31356438	GM12878	blood:	n/a	chr16:31356243-31356252
35	BHLHE40	chr16:31345088-31345267	GM12878	blood:	n/a	n/a
36	BHLHE40	chr16:31369123-31369374	GM12878	blood:	n/a	n/a
37	BHLHE40	chr16:31382864-31383366	HepG2	liver:	n/a	n/a
38	BHLHE40	chr16:31397666-31397921	K562	blood:	n/a	n/a
39	BHLHE40	chr16:31365765-31366540	GM12878	blood:	n/a	n/a
40	BHLHE40	chr16:31366209-31366562	K562	blood:	n/a	n/a
41	BHLHE40	chr16:31405046-31405194	K562	blood:	n/a	chr16:31405138-31405159 chr16:31405145-31405154
42	BHLHE40	chr16:31343252-31343457	K562	blood:	n/a	n/a
43	BHLHE40	chr16:31362869-31363241	GM12878	blood:	n/a	n/a
44	BHLHE40	chr16:31363583-31363831	GM12878	blood:	n/a	n/a
45	BHLHE40	chr16:31393969-31394197	K562	blood:	n/a	n/a
46	BHLHE40	chr16:31339290-31339349	K562	blood:	n/a	n/a
47	BHLHE40	chr16:31356051-31356453	GM12878	blood:	n/a	n/a
48	BHLHE40	chr16:31345064-31345232	K562	blood:	n/a	n/a
49	BHLHE40	chr16:31376441-31376816	GM12878	blood:	n/a	n/a
50	BRCA1	chr16:31345131-31345191	HepG2	liver:	n/a	n/a

(count:2077 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:31343428-31343478	K562	blood:	n/a
2	chr16:31342453-31342503	PrEC	prostate:	n/a
3	chr16:31345277-31345327	AG09319	gingival:	n/a
4	chr16:31343428-31343478	K562	blood:	n/a
5	chr16:31342453-31342503	PrEC	prostate:	n/a
6	chr16:31345277-31345327	AG09319	gingival:	n/a
7	chr16:31340340-31340390	HCM	heart:	n/a
8	chr16:31342453-31342503	Jurkat	blood:	n/a
9	chr16:31383800-31383850	HEK293	kidney:	embryo
10	chr16:31383800-31383850	GM06990	blood:	n/a
11	chr16:31340805-31340855	ECC-1	luminal epithelium:	n/a
12	chr16:31366418-31366468	SKMC	muscle:	n/a
13	chr16:31366377-31366427	HepG2	liver:	n/a
14	chr16:31408898-31408948	AG04449	skin:	fetal
15	chr16:31383689-31383739	T-47D	breast:	n/a
16	chr16:31342952-31343002	GM06990	blood:	n/a
17	chr16:31366377-31366427	PrEC	prostate:	n/a
18	chr16:31366377-31366427	NHBE	bronchial:	n/a
19	chr16:31366536-31366586	RPTEC	kidney:	n/a
20	chr16:31343056-31343106	AG10803	skin:	n/a
21	chr16:31385282-31385332	Jurkat	blood:	n/a
22	chr16:31382930-31382980	A549	lung:	n/a
23	chr16:31366418-31366468	HL-60	blood:	n/a
24	chr16:31342453-31342503	NB4	blood:	n/a
25	chr16:31383049-31383099	AoSMC	blood vessel:	n/a
26	chr16:31384854-31384904	Jurkat	blood:	n/a
27	chr16:31408867-31408917	MCF-7	breast:	n/a
28	chr16:31366429-31366479	PFSK-1	brain:	n/a
29	chr16:31394096-31394146	HCPEpiC	choroid plexus:	n/a
30	chr16:31408898-31408948	GM12891	blood:	n/a
31	chr16:31382930-31382980	HCT-116	colon:	n/a
32	chr16:31342952-31343002	HUVEC	blood vessel:	n/a
33	chr16:31342748-31342798	BE2_C	brain:	n/a
34	chr16:31384854-31384904	NB4	blood:	n/a
35	chr16:31383689-31383739	HUVEC	blood vessel:	n/a
36	chr16:31408712-31408762	HPAEpiC	pulmonary alveolar:	n/a
37	chr16:31366118-31366168	H1-hESC	embryonic stem cell:	embryo
38	chr16:31408900-31408950	BJ	skin:	n/a
39	chr16:31366418-31366468	SK-N-SH	brain:	n/a
40	chr16:31342952-31343002	HCF	heart:	n/a
41	chr16:31342748-31342798	AG10803	skin:	n/a
42	chr16:31342748-31342798	NHBE	bronchial:	n/a
43	chr16:31340805-31340855	GM12891	blood:	n/a
44	chr16:31383800-31383850	GM12892	blood:	n/a
45	chr16:31385282-31385332	SK-N-MC	brain:	n/a
46	chr16:31408900-31408950	AG04450	lung:	fetal
47	chr16:31384854-31384904	GM19239	blood:	n/a
48	chr16:31341479-31341529	NHBE	bronchial:	n/a
49	chr16:31383642-31383692	T-47D	breast:	n/a
50	chr16:31383049-31383099	Hepatocyte	liver:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:31404071..31406519-chr16:31413482..31415617,2	K562	blood:
2	chr16:31393820..31395534-chr16:31395638..31397833,2	MCF-7	breast:
3	chr16:30996013..30996554-chr16:31393734..31394639,2	MCF-7	breast:
4	chr16:31370114..31372263-chr16:31373641..31375780,2	MCF-7	breast:
5	chr16:31405158..31408011-chr16:31425171..31426679,2	MCF-7	breast:
6	chr16:31340966..31343264-chr16:31454013..31455624,2	MCF-7	breast:
7	chr16:31191136..31192870-chr16:31404226..31406023,2	MCF-7	breast:
8	chr16:31404071..31406519-chr16:31413482..31415617,2	K562	blood:
9	chr16:31396941..31397680-chr16:31454467..31454971,2	MCF-7	breast:
10	chr16:31145768..31147739-chr16:31345988..31347524,2	MCF-7	breast:
11	chr16:31191175..31193131-chr16:31364382..31367193,2	K562	blood:
12	chr16:31190368..31193316-chr16:31342467..31345225,2	K562	blood:
13	chr16:30996739..30997303-chr16:31344859..31345633,2	MCF-7	breast:
14	chr16:31341937..31343785-chr16:31345527..31347045,2	K562	blood:
15	chr16:31409305..31411632-chr16:31412830..31415079,2	K562	blood:
16	chr16:31118693..31121313-chr16:31341607..31344535,2	MCF-7	breast:
17	chr16:31397034..31399746-chr16:31400566..31403518,3	MCF-7	breast:
18	chr16:31400836..31402888-chr16:31406431..31408279,2	MCF-7	breast:
19	chr16:31083852..31086357-chr16:31391531..31394132,2	MCF-7	breast:
20	chr16:31384535..31387271-chr16:31390776..31392528,2	K562	blood:
21	chr16:31375617..31378307-chr16:31436876..31438549,2	K562	blood:
22	chr16:31211282..31213179-chr16:31343243..31345626,2	K562	blood:
23	chr16:31364585..31367756-chr16:31369594..31371710,3	K562	blood:
24	chr16:31375595..31378224-chr16:31462241..31464094,2	K562	blood:
25	chr16:31365891..31370863-chr16:31373415..31376025,5	K562	blood:
26	chr16:31397034..31399746-chr16:31400566..31403518,3	MCF-7	breast:
27	chr16:31383689..31387249-chr16:31389640..31393278,4	MCF-7	breast:
28	chr16:31400836..31402888-chr16:31406431..31408279,2	MCF-7	breast:
29	chr16:31198991..31202851-chr16:31343045..31346880,4	K562	blood:
30	chr16:31190461..31193356-chr16:31392398..31395523,4	MCF-7	breast:
31	chr16:31277354..31279123-chr16:31386199..31389124,2	K562	blood:
32	chr16:31190461..31191992-chr16:31356554..31358411,2	MCF-7	breast:
33	chr16:30999038..31001529-chr16:31346351..31348185,2	K562	blood:
34	chr16:31189640..31192983-chr16:31385615..31388783,3	MCF-7	breast:
35	chr16:31342392..31343986-chr16:31347244..31349142,2	MCF-7	breast:
36	chr16:31190410..31192948-chr16:31385235..31387421,2	MCF-7	breast:
37	chr16:31393820..31395534-chr16:31395638..31397833,2	MCF-7	breast:
38	chr16:31364585..31367756-chr16:31369594..31371710,3	K562	blood:
39	chr16:31383533..31386035-chr16:31390623..31392276,2	K562	blood:
40	chr16:31190496..31192214-chr16:31368075..31369676,2	MCF-7	breast:
41	chr16:31373565..31374565-chr20:49341478..49342019,2	MCF-7	breast:
42	chr16:31360694..31362318-chr16:31366336..31368356,2	K562	blood:
43	chr16:31360184..31362565-chr16:31363360..31366821,3	MCF-7	breast:
44	chr16:31407031..31409416-chr16:31465348..31468192,2	MCF-7	breast:
45	chr16:31212227..31213115-chr16:31344705..31345602,3	MCF-7	breast:
46	chr16:31383689..31387249-chr16:31389640..31393278,4	MCF-7	breast:
47	chr16:31366361..31368060-chr16:31368172..31370932,2	MCF-7	breast:
48	chr16:31408712..31410722-chr16:31883758..31886436,2	K562	blood:
49	chr16:31370070..31372965-chr16:31413920..31417255,3	K562	blood:
50	chr16:31383533..31386035-chr16:31390623..31392276,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COX6A2-3	chr16:31369774-31370107	expReg_chr16_4465_-
2	lnc-COX6A2-5	chr16:31340255-31340277	NONHSAT141893
3	lnc-ITGAX-2	chr16:31367214-31367599	NONHSAT141895
4	lnc-COX6A2-4	chr16:31343328-31344118	NONHSAT141894
5	lnc-ITGAX-2	chr16:31367946-31368049	NONHSAT141896
6	lnc-COX6A2-2	chr16:31372860-31373016	NONHSAT141897
7	lnc-ITGAX-1	chr16:31414558-31416020	ENSG00000260757.1
8	lnc-COX6A2-4	chr16:31343127-31343183	NONHSAT141894
9	lnc-COX6A2-2	chr16:31372599-31372774	NONHSAT141897
10	lnc-ITGAX-2	chr16:31366509-31366612	NONHSAT141896
11	lnc-COX6A2-5	chr16:31338997-31340036	NONHSAT141893
12	lnc-ITGAX-1	chr16:31413886-31414189	ENSG00000260757.1
13	lnc-ITGAX-2	chr16:31367214-31367319	NONHSAT141896
14	lnc-ITGAX-2	chr16:31366455-31366612	NONHSAT141895
15	lnc-ITGAX-2	chr16:31368352-31369183	NONHSAT141896

No data

Variant related genes	Relation type
ENSG00000261245	TF binding region
ITGAM	TF binding region
ITGAX	TF binding region
ENSG00000260757	TF binding region
ITGAD	TF binding region
ENSG00000261245	CpG island
ITGAM	CpG island
ITGAX	CpG island
ENSG00000260757	CpG island
ITGAD	CpG island
ENSG00000099377	chromatin interactions
ENSG00000167394	chromatin interactions
ENSG00000176723	chromatin interactions
ENSG00000140691	chromatin interactions
ENSG00000167395	chromatin interactions
ENSG00000156886	chromatin interactions
ENSG00000185947	chromatin interactions
ENSG00000169896	chromatin interactions
ENSG00000252876	chromatin interactions
ENSG00000261359	chromatin interactions
ENSG00000169900	chromatin interactions
ENSG00000260267	chromatin interactions
ENSG00000140678	chromatin interactions
ENSG00000052344	chromatin interactions
ENSG00000177238	chromatin interactions
ENSG00000252809	chromatin interactions
ENSG00000103507	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000260757	chromatin interactions

Extended variants
information (count: 3304 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:3304 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376900371	chr16:31337465-31337466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537165898	chr16:31337466-31337467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543001280	chr16:31337477-31337478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537161168	chr16:31337504-31337505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs41371846	chr16:31337528-31337529	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs41413245	chr16:31337531-31337532	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs564680668	chr16:31337536-31337537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181991735	chr16:31337545-31337546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528889252	chr16:31337631-31337632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572314095	chr16:31337632-31337633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs41440449	chr16:31337677-31337678	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs374721393	chr16:31337679-31337680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185232834	chr16:31337687-31337688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543570696	chr16:31337691-31337692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541270768	chr16:31337719-31337720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199505424	chr16:31337720-31337721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559857225	chr16:31337750-31337751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191167661	chr16:31337774-31337775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112638876	chr16:31337792-31337793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529553739	chr16:31337799-31337800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547980707	chr16:31337873-31337874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs41474849	chr16:31337886-31337887	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs368058466	chr16:31337917-31337918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533704367	chr16:31338027-31338028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182961442	chr16:31338028-31338029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569746739	chr16:31338038-31338039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186766591	chr16:31338114-31338115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374482702	chr16:31338167-31338168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371481891	chr16:31338170-31338171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377439961	chr16:31338194-31338195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371245740	chr16:31338218-31338219	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs535254188	chr16:31338228-31338229	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs553934657	chr16:31338248-31338249	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs548836661	chr16:31338253-31338254	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs374240979	chr16:31338265-31338266	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs565808303	chr16:31338287-31338288	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs377138770	chr16:31338291-31338292	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs557765166	chr16:31338294-31338295	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs576154262	chr16:31338427-31338428	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191208562	chr16:31338468-31338469	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555461789	chr16:31338549-31338550	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573686153	chr16:31338566-31338567	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541240262	chr16:31338603-31338604	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149223988	chr16:31338630-31338631	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533444781	chr16:31338647-31338648	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375609232	chr16:31338660-31338661	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs76939857	chr16:31338691-31338692	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71151472	chr16:31338745-31338746	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146897993	chr16:31338840-31338841	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7192375	chr16:31338938-31338939	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:121)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:994 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31323000-31344600	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr16:31331800-31342000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr16:31332200-31342000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr16:31333600-31339600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr16:31333600-31342400	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr16:31333800-31342400	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr16:31334000-31338200	Weak transcription	Primary B cells from cord blood	blood
8	chr16:31334600-31339600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr16:31335200-31341800	Weak transcription	Primary B cells from peripheral blood	blood
10	chr16:31335800-31342000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr16:31336800-31338800	Weak transcription	Spleen	Spleen
12	chr16:31336800-31339600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr16:31337000-31340800	Weak transcription	Placenta	Placenta
14	chr16:31337200-31338200	Weak transcription	Lung	lung
15	chr16:31337200-31338600	Weak transcription	Adipose Nuclei	Adipose
16	chr16:31338200-31338400	ZNF genes & repeats	Gastric	stomach
17	chr16:31338200-31338400	ZNF genes & repeats	Lung	lung
18	chr16:31338200-31340200	Strong transcription	Primary B cells from cord blood	blood
19	chr16:31338400-31339400	Enhancers	Thymus	Thymus
20	chr16:31338400-31342600	Weak transcription	Gastric	stomach
21	chr16:31338800-31342000	Strong transcription	Spleen	Spleen
22	chr16:31339000-31339200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr16:31339000-31339400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr16:31339000-31339400	Enhancers	Fetal Thymus	thymus
25	chr16:31339000-31340000	Enhancers	GM12878-XiMat	blood
26	chr16:31339000-31340200	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr16:31339000-31340200	Enhancers	Dnd41	blood
28	chr16:31339200-31339600	Enhancers	H1 Cell Line	embryonic stem cell
29	chr16:31339200-31339800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr16:31339200-31340000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr16:31339200-31340000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr16:31339400-31339600	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr16:31339400-31339600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr16:31339400-31339600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr16:31339400-31339800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr16:31339400-31339800	Flanking Active TSS	Fetal Thymus	thymus
37	chr16:31339400-31339800	Flanking Active TSS	Thymus	Thymus
38	chr16:31339400-31340000	Enhancers	K562	blood
39	chr16:31339400-31340200	Enhancers	Primary hematopoietic stem cells	blood
40	chr16:31339600-31339800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr16:31339600-31339800	Enhancers	H9 Cell Line	embryonic stem cell
42	chr16:31339600-31339800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
43	chr16:31339600-31339800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr16:31339600-31340000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
45	chr16:31339600-31340000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr16:31339600-31340800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr16:31339800-31340000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr16:31339800-31340000	Bivalent/Poised TSS	Fetal Heart	heart
49	chr16:31339800-31340000	Active TSS	Fetal Thymus	thymus
50	chr16:31339800-31340200	Bivalent Enhancer	Duodenum Mucosa	Duodenum

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